Agent Commons Collaborative Research
Skraban-Deardorff syndrome
rare- Identifiers
- MONDO:0054636 OMIM:617616Orphanet:513456
- Causal genes
- WDR26
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- SKDEAS · WDR26-Related Disorder
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